Neoplasma. 2016;63(1):64-71. doi: 10.4149/neo_2016_008.
The purpose of this study was to investigate the potential role of Ileucyl-tRNA synthetase (IARS2) silencing in non-small cell lung cancer (NSCLC). The silencing of IARS2 in H1299 cells and A549 cells were performed by lentivirus encoding shRNAs. The efficiency of IARS2 silencing was detected by quantitative real time PCR and western blot. The effects of IARS2 silencing on cell growth, cell apoptosis, cell cycle and cell colony formation ability were assessed by cells counting, MTT assay, flow cytometer analysis and soft agar colony formation assay, respectively. Compared with negative control group, IARS2 was significantly knockdown by transfection with lentivirus encoding shRNA of IARS2. The IARS2 silencing significantly inhibited the cells proliferation and cells colony formation ability, induced cell cycle arrest at G1/S phase and promoted cell apoptosis. IARS2 silencing induced NSCLC cells growth inhibition, cell cycle arrest and promoted cell apoptosis. These results suggest that IARS2 may be a novel target for the treatment of NSCLC.
本研究旨在探讨亮氨酰-tRNA 合成酶(IARS2)沉默在非小细胞肺癌(NSCLC)中的潜在作用。通过慢病毒编码 shRNA 沉默 H1299 细胞和 A549 细胞中的 IARS2。通过定量实时 PCR 和 Western blot 检测 IARS2 沉默的效率。通过细胞计数、MTT 测定、流式细胞仪分析和软琼脂集落形成测定分别评估 IARS2 沉默对细胞生长、细胞凋亡、细胞周期和细胞集落形成能力的影响。与阴性对照组相比,用编码 IARS2 shRNA 的慢病毒转染可显著敲低 IARS2。IARS2 沉默显著抑制细胞增殖和细胞集落形成能力,诱导细胞周期停滞在 G1/S 期并促进细胞凋亡。IARS2 沉默诱导 NSCLC 细胞生长抑制、细胞周期停滞和促进细胞凋亡。这些结果表明,IARS2 可能是治疗 NSCLC 的一个新靶点。